2,4-dinitro-6-(1-methylheptyl)phenol

2,4-dinitro-6-(1-methylheptyl)phenol Structure
CAS No.
3687-22-7
Chemical Name:
2,4-dinitro-6-(1-methylheptyl)phenol
Synonyms
Clonidine Impurity 16;DNOP (technical mixture);2,4-dinitro-6-(oct-2-yl)phenol;2,4-Dinitro-6-(octan-2-yl)phenol;2,4-dinitro-6-(1-methylheptyl)phenol;Phenol, 2-(1-methylheptyl)-4,6-dinitro-;2,4-Dinitro-6-(octan-2-yl)phenol Solution, 100ppm;2,4-Dinitro-6-(octan-2-yl)phenol Solution in Acetonitrile, 100μg/mL
CBNumber:
CB12470882
Molecular Formula:
C14H20N2O5
Molecular Weight:
296.32
MOL File:
3687-22-7.mol
Modify Date:
2023/5/15 10:43:59

2,4-dinitro-6-(1-methylheptyl)phenol Properties

Density 1.16 at 21℃
vapor pressure 0.005Pa at 25℃
solubility Chloroform (Slightly), Methanol (Slightly)
form Oil
color Light Yellow to Yellow
Stability Stability
LogP 6.27
Dissociation constant 5.69-6.79 at 25℃
CAS DataBase Reference 3687-22-7
EPA Substance Registry System 2,4-Dinitro-6-(1-methylheptyl)phenol (3687-22-7)

2,4-dinitro-6-(1-methylheptyl)phenol Chemical Properties,Uses,Production

Reactivity Profile

2,4-dinitro-6-(1-methylheptyl)phenol is an organonitrate/phenol. Organonitrate compounds range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups. Phenols do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases.

Fire Hazard

Flash point data for 2,4-dinitro-6-(1-methylheptyl)phenol are not available. 2,4-dinitro-6-(1-methylheptyl)phenol is probably combustible.

2,4-dinitro-6-(1-methylheptyl)phenol Preparation Products And Raw materials

2,4-dinitro-6-(1-methylheptyl)phenol 2,4-Dinitro-6-(octan-2-yl)phenol Solution, 100ppm 2,4-dinitro-6-(oct-2-yl)phenol DNOP (technical mixture) Phenol, 2-(1-methylheptyl)-4,6-dinitro- 2,4-Dinitro-6-(octan-2-yl)phenol Solution in Acetonitrile, 100μg/mL 2,4-Dinitro-6-(octan-2-yl)phenol Clonidine Impurity 16 3687-22-7